Related Experiment Videos
A controlled spinal cord contusion for the rhesus macaque monkey
Zhengwen Ma1, Yi Ping Zhang2, Wei Liu1
1Department of Laboratory Animal Sciences, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, PR China.
Experimental Neurology
|February 16, 2016
Summary
Researchers developed a new non-human primate model for spinal cord injury (SCI). This primate model shows severity-dependent deficits, aiding the translation of SCI repair strategies to human clinical applications.
Area of Science:
- Neuroscience
- Regenerative Medicine
- Animal Models
Background:
- Rodent models of spinal cord injury (SCI) have limitations due to anatomical and functional differences with humans.
- There is a critical need for large animal models, like non-human primates, to bridge the gap between laboratory research and clinical applications for SCI.
Purpose of the Study:
- To establish a controlled, clinically-relevant contusive spinal cord injury model in non-human primates.
- To characterize the severity-dependent functional and histological outcomes of this new SCI model.
Main Methods:
- Adult male rhesus macaques underwent mild to moderate contusive SCI (1.0 or 1.5mm tissue displacement) or sham laminectomy.
- Functional assessments included motor-evoked potentials (MEP), somatosensory-evoked potentials (SSEP), and the monkey hindlimb score (MHS).
- MR imaging (including DTI tractography) and histological analysis of lesion sites were performed at various time points up to 6 months post-injury.
Main Results:
- The monkey hindlimb score demonstrated severity-dependent neurological deficits.
- MEP response rates were depressed or abolished, and SSEP showed slight decreases post-injury.
- MRI revealed lesion site changes, DTI showed interrupted fiber tracts, and histology confirmed severity-dependent spinal cord atrophy, axonal degeneration, and myelin loss.
Conclusions:
- A reproducible, severity-dependent contusive spinal cord injury model was established in non-human primates.
- This model exhibits functional and histological deficits relevant to human SCI, potentially facilitating the translation of therapeutic strategies.
- The absence of strong astrocytic gliosis in the lesion penumbra of this model warrants further investigation.